inborn disorder of bilirubin metabolism
Go to external page http://purl.obolibrary.org/obo/MONDO_0017755
An instance of bilirubin metabolism disease that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]
Synonyms: hereditary bilirubin metabolism disease disorder of bilirubin metabolism and excretion inborn disorder of bilirubin metabolism and excretion
Term information
- icd11.foundation:1297666279 (https://orcid.org/0000-0002-4142-7153)
- MEDGEN:1671515 (MONDO:equivalentTo)
- GARD:21347 (MONDO:GARD)
- Orphanet:309816 (MONDO:equivalentTo)
- UMLS:C0349427 (MONDO:equivalentTo)
gard_rare, disease_grouping, rare, ordo_group_of_disorders
http://www.orpha.net/ORDO/Orphanet_309816
http://identifiers.org/medgen/1671515
http://linkedlifedata.com/resource/umls/id/C0349427